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Research Article

Tuning the spectral, thermal and morphological properties of Poly(o-phenylenediamine-co-vaniline)

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Pages 25-35 | Received 03 Nov 2020, Accepted 23 Dec 2020, Published online: 05 Jan 2021

References

  • Jadoun S, Riaz U, Budhiraja V. Biodegradable conducting polymeric materials for biomedical applications: a review. Med Dev Sen. 2020. DOI:https://doi.org/10.1002/mds3.10141.
  • Khokhar D, Jadoun S, Arif R, et al. Functionalization of conducting polymers and their applications in optoelectronics. Polym Plast Technol Eng. 2020:1–23. DOI:https://doi.org/10.1080/25740881.2020.1819312.
  • Kumari Jangid N, Jadoun S, Kaur N. A review on high-throughput synthesis, deposition of thin films and properties of polyaniline. Eur Polym J. 2020;125:109485.
  • Jangid NK, Jadoun S, Yadav A, et al. Polyaniline-TiO2-based photocatalysts for dyes degradation. Polym Bull. 2020. DOI:https://doi.org/10.1007/s00289-020-03318-w.
  • Waware US, Hamouda AMS, Poly RM. (aniline-co-2-hydroxyaniline): towards the thermal stability and higher solubility of polyaniline. Appl Phys A. 2019;125:127.
  • Gicevicius M, Kucinski J, Ramanaviciene A, et al. Tuning the optical pH sensing properties of polyaniline-based layer by electrochemical copolymerization of aniline with o-phenylenediamine. Dyes Pigm. 2019;170:107457.
  • Khodadadi A, Faghih-Mirzaei E, Karimi-Maleh H, et al. A new epirubicin biosensor based on amplifying DNA interactions with polypyrrole and nitrogen-doped reduced graphene: experimental and docking theoretical investigations. Sens Actuators B Chem. 2019;284:568–574.
  • Sabury S, Collier GS, Ericson MN, et al. Synthesis of a soluble adenine-functionalized polythiophene through direct arylation polymerization and its fluorescence responsive behavior. Polym Chem. 2020;11(4):820–829. .
  • Hsieh H-C, Hsiow C-Y, Su Y-A, et al. Two-dimensional polythiophene homopolymer as promising hole transport material for high-performance perovskite solar cells. J Power Sources. 2019;426:55–60.
  • Young CA, Hammack A, Lee HJ, et al. Poly (1, 4-phenylene vinylene) derivatives with ether substituents to improve polymer solubility for use in organic light-emitting diode devices. ACS Omega. 2019;4(27):22332–22344.
  • Riaz U, Ashraf SM, Fatima T, et al. Tuning the spectral, morphological and photophysical properties of sonochemically synthesized poly(carbazole) using acid Orange, fluorescein and rhodamine 6G. Spectrochim Acta A Mol Biomol Spectrosc. 2017;173.
  • Riaz U, Ashraf SM, Kumar Saroj S, et al. Microwave-assisted solid state intercalation of Rhodamine B and polycarbazole in bentonite clay interlayer space: structural characterization and photophysics of double intercalation. RSC Adv. 2016;6.
  • Jadoun S, Verma A, Ashraf SM, et al. A short review on the synthesis, characterization, and application studies of poly(1-naphthylamine): a seldom explored polyaniline derivative. Colloid Polym Sci. 2017;295(9):1443–1453.
  • Zoromba MS, Al-Hossainy AF. Doped poly (o-phenylenediamine-co-p-toluidine) fibers for polymer solar cells applications. Solar Energy. 2020;195:194–209.
  • Riaz U, Jadoun S, Kumar P, et al. Microwave-assisted facile synthesis of poly(luminol-co -phenylenediamine) copolymers and their potential application in biomedical imaging. RSC Adv. 2018;8:37165–37175.
  • Fache M, Boutevin B, Caillol S. Vanillin, a key-intermediate of biobased polymers. Eur Polym J. 2015;68:488–502.
  • Llevot A, Grau E, Carlotti S, et al. From lignin‐derived aromatic compounds to novel biobased polymers. Macromol Rapid Commun. 2016;37:9–28.
  • Fache M, Darroman E, Besse V, et al. Vanillin, a promising biobased building-block for monomer synthesis. Green Chem. 2014;16:1987–1998.
  • Abdelaty MSA. Preparation and characterization of new environmental functional polymers based on vanillin and N-isopropylacrylamide for post polymerization. J Polym Environ. 2018;26:636–646.
  • Stroescu M, Stoica-Guzun A, Isopencu G, et al. Chitosan-vanillin composites with antimicrobial properties. Food Hydrocoll. 2015;48:62–71.
  • Turan N, Buldurun K, Alan Y, et al. Synthesis, characterization, antioxidant, antimicrobial and DNA binding properties of ruthenium (II), cobalt (II) and nickel (II) complexes of Schiff base containing o-vanillin. Res Chem Intermed. 2019;45:3525–3540.
  • L V K, Sunitha S, Nath GR. Antioxidant, antidiabetic and anticancer studies of nickel complex of Vanillin-4-methyl-4-phenyl-3-thiosemicarbazone. Mater Today Proc. 2020.
  • Bhargava S, Uma V. Rapid extraction of Cu (II) heavy metal from industrial waste water by using silver nanoparticles anchored with novel Schiff base. Sep Sci Technol. 2019;54:1182–1193.
  • Amarasekara AS, Razzaq A. Vanillin-based polymers—part II: synthesis of Schiff base polymers of divanillin and their chelation with metal ions. Int Sch Res Notices. 2012;2012.
  • Satpati S, Saha SK, Suhasaria A, et al. Adsorption and anti-corrosion characteristics of vanillin Schiff bases on mild steel in 1 M HCl: experimental and theoretical study. RSC Adv. 2020;10:9258–9273.
  • Dineshkumar S, Muthusamy A. Investigation of aggregation induced emission in 4-hydroxy-3-methoxybenzaldehyde azine and polyazine towards application in (opto) electronics: synthesis, characterization, photophysical and electrical properties. Des Monomers Polym. 2017;20:234–249.
  • Zaltariov M-F, Cazacu M, Avadanei M, et al. Synthesis, characterization and antimicrobial activity of new Cu (II) and Zn (II) complexes with Schiff bases derived from trimethylsilyl-propyl-p-aminobenzoate. Polyhedron. 2015;100:121–131.
  • Riaz U, Ashraf SM, Aleem S, et al. Microwave-assisted green synthesis of some nanoconjugated copolymers: characterisation and fluorescence quenching studies with bovine serum albumin. New J Chem. 2016;40.
  • Jadoun S, Sharma V, Ashraf SM, et al. Sonolytic doping of poly(1-naphthylamine) with luminol: influence on spectral, morphological and fluorescent characteristics. Colloid Polym Sci. 2017;295:715–724.
  • Jadoun S, Ashraf SM, Riaz U. Tuning the spectral, thermal and fluorescent properties of conjugated polymers: via random copolymerization of hole transporting monomers. RSC Adv. 2017;7:32757–32768.
  • Huang MM-R, Li XX-G, Duan W, et al. Evaluation of antibacterial activity of nanostructured copolymers of poly (Naphthylamine). Synth Met [Internet]. 2016;4:406–410.
  • Miliauskas G, Venskutonis PR, van Beek TA. Screening of radical scavenging activity of some medicinal and aromatic plant extracts. Food Chem. 2004;85:231–237.
  • Vishal RP, Rakesh KP. In vivo anti-oxidant activity of Dhatrinisha churna and Manjisthadi churna in high fat diet induced oxidative stress. Free Radicals Antioxid. 2012;2:19–23.
  • Mistry B, Patel RV, Keum Y-S. Access to the substituted benzyl-1,2,3-triazolyl hesperetin derivatives expressing antioxidant and anticancer effects. Arabian J Chem. 2017;10:157–166.
  • Ruch RJ, Cheng S, Klaunig JE. Prevention of cytotoxicity and inhibition of intercellular communication by antioxidant catechins isolated from Chinese green tea. Carcinogenesis. 1989;10:1003–1008.
  • Jadoun S, Biswal L, Riaz U. Tuning the optical properties of poly(o-phenylenediamine-co-pyrrole) via template mediated copolymerization. Des Monomers Polym. 2018;21:75–81.
  • Riaz U, Jadoun S, Kumar P, et al. Influence of Luminol doping of poly(o-phenylenediamine) on the spectral, morphological and fluorescent properties: A potential biomarker for Leishmania parasite. ACS Appl Mater Interfaces. 2017;acsami.7b10325.
  • Riaz U, Ashraf SM. Microwave-assisted solid state in situ polymerization and intercalation of poly(carbazole) between bentonite layers: effect of microwave irradiation and gallery confinement on the spectral, fluorescent, and morphological properties. J Phys Chem C. 2012;116:12366–12374.
  • Gutzler R. Band-structure engineering in conjugated 2D polymers. Phys Chem Chem Phys. 2016;18:29092–29100.
  • Xu C, Wright M, Elumalai NK, et al. Optimization of conjugated polymer blend concentration for high performance organic solar cells. J Mater Sci. 2018;29:16437–16445.
  • Zhou K, Yu L. Effects of extraction solvent on wheat bran antioxidant activity estimation. LWT - Food Sc Technol. 2004;37:717–721.
  • Ansari IA, Sama F, Shahid M, et al. Isolation of proton transfer complexes containing 4-picolinium as cation and pyridine-2,6-dicarboxylate complex as anion: crystallographic and spectral investigations, antioxidant activities and molecular docking studies. RSC Adv. 2016;6:11088–11098.
  • Arif R, Nayab PS, Ansari IA, et al. Synthesis, molecular docking and DNA binding studies of phthalimide-based copper(II) complex: in vitro antibacterial, hemolytic and antioxidant assessment. J Mol Struct. 2018;1160:142–153.

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